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Up and Up Childrens all day allergy relief - 11673-974-34 - (cetirizine hydrochloride)

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Drug Information of Up and Up Childrens all day allergy relief

Product NDC: 11673-974
Proprietary Name: Up and Up Childrens all day allergy relief
Non Proprietary Name: cetirizine hydrochloride
Active Ingredient(s): 5    mg/5mL & nbsp;   cetirizine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Up and Up Childrens all day allergy relief

Product NDC: 11673-974
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090254
Marketing Category: ANDA
Start Marketing Date: 20090612

Package Information of Up and Up Childrens all day allergy relief

Package NDC: 11673-974-34
Package Description: 1 BOTTLE in 1 CARTON (11673-974-34) > 236 mL in 1 BOTTLE

NDC Information of Up and Up Childrens all day allergy relief

NDC Code 11673-974-34
Proprietary Name Up and Up Childrens all day allergy relief
Package Description 1 BOTTLE in 1 CARTON (11673-974-34) > 236 mL in 1 BOTTLE
Product NDC 11673-974
Product Type Name HUMAN OTC DRUG
Non Proprietary Name cetirizine hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20090612
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Up and Up Childrens all day allergy relief


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